Canonical Allele Identifier: CA1979406086
Gene: OVOL1 HGNC NCBI

Linked Data

dbSNP Id: rs1858024882
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65791842_65791843del , CM000673.2:g.65791842_65791843del GRCh38
NC_000011.9:g.65559313_65559314del , CM000673.1:g.65559313_65559314del GRCh37
NC_000011.8:g.65315889_65315890del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000335987.8:c.101-2189_101-2188del MANE Select ENSP00000337862.3:n.101-2189_101-2188del
ENST00000335987.7:c.101-2189_101-2188del ENSP00000337862.3:n.101-2189_101-2188del
ENST00000531907.1:n.361-476_361-475del
NM_004561.3:c.101-2189_101-2188del NP_004552.2:n.101-2189_101-2188del
XM_005274018.3:c.-87+2149_-87+2150del XP_005274075.1:n.-87+2149_-87+2150del
XM_011545067.1:c.-86-2189_-86-2188del XP_011543369.1:n.-86-2189_-86-2188del
XM_011545068.1:c.-87+979_-87+980del XP_011543370.1:n.-87+979_-87+980del
XM_011545067.2:c.-86-2189_-86-2188del XP_011543369.1:n.-86-2189_-86-2188del
XM_011545068.3:c.-87+979_-87+980del XP_011543370.1:n.-87+979_-87+980del
XM_017017837.1:c.-86-2189_-86-2188del XP_016873326.1:n.-86-2189_-86-2188del
NM_004561.4:c.101-2189_101-2188del MANE Select NP_004552.2:n.101-2189_101-2188del
Search 100 bp 5'
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